CClinicalTrials.gg
Active, not recruitingNCT02611570Updated Oct 30, 2024

LDCT Screening in Non-smokers in Taiwan

An observational study in Lung Cancer, sponsored by Academia Sinica, Taiwan. Active, not recruiting at 17 sites in Taiwan. Open to participants aged Up to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-10-30.

Sponsored by Academia Sinica, Taiwan · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
12,000
Ages
Up to 75 Years
Sex
All
01

Study summary

This study utilizes the low dose computed tomography(LDCT) to detect the occurrence of early lung cancer among non-smokers in Taiwan. Subjects who have family history of lung cancer or have high risk exposures to lung cancer will be recruited to participate LDCT screening and followed up for their possible occurrence of lung cancer.

Read the detailed description

Lung cancer ranks the No. 1 lethal cancer in Taiwan, with a five-year survival rate (5-yr SR) of only 15%. Most of the patients with early lung cancer are asymptomatic, while 75% of patients with cancer-related symptom at diagnosis have local or distant metastasis. Compared to a 5-yr SR of 70-90% in stage I/II lung cancer, the 5-yr SR in late stage IIIb/IV is less than 15%. Despite the progress in pharmaceutical treatment for late stage disease, early detection is still the only way to improve the outcome and even cure of this potentially lethal disease. Low dose computed tomography (LDCT) in recognized as the best tool available for early diagnosis of lung cancer. However, the radiation exposure, high cost and high false-positive rate are the major concerns to adapt this detection tool to general population. Recent studies from Europe and US have shown that LDCT screening in high-risk cigarette smoking population can effectively reduce lung cancer mortality. However, the major type of lung cancer in Taiwan is adenocarcinoma, which commonly occurs in non-smoker. Therefore, the risk prediction model generated from studies of western countries may not be suitable for directly adapted to our country. LDCT screening for lung cancer detection in non-smoker remains a controversial issue worldwide, including Taiwan. Facing the unmet need, it is urgent to establish the risk assessment model to predict lung cancer risks in non-smokers and to evaluate the efficacy of LDCT screening in non-smoker high-risk population. In this study, we plan to enroll 12000 non-smoker subjects with a given lung cancer risk; half of them should have lung cancer family history. Each participant will receive LDCT at baseline, annually for two years, and biennially for 6 years. Our overall goal is to establish a risk assessment model of lung cancer in non-smokers and provide suggestions to government for considerations for lung cancer prevention and screening policy in Taiwan.

There are three specific aims in our proposed study:

Aim 1: To evaluate the risk assessment model for predicting lung cancer in non-smokers According to the results of LDCT screening, we expect to improve the risk prediction model for nonsmoker female established by GELAC study. The revised risk model will help recognizing higher risk population.

Aim 2: To establish the protocol for LDCT screening pilot study in Taiwan Establishing working protocol and procedures of LDCT screening to assure a homogeneous behavior among study sites

Aim 3: To establish the efficacy of LDCT screening for lung cancer in non-smoker Lung cancer detection rate, false-positive rate, and cost-effectiveness analysis of LDCT screening for non-smoker lung cancer in Taiwan will be established.

02

Conditions studied

  • Lung Cancer

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Keywords

  • Lung cancer
  • Low dose computed tomography
  • Screening
  • Non-smoker
  • Gender issue
03

In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's planned enrollment of 12,000 is above the median of 189 across 1,514 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Academia Sinica, Taiwan is the lead sponsor of 14 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

High risk population for lung cancer

Inclusion criteria

  1. Never smokers or have smoked less than 10 pack-years and quitted smoking over 15 years.
  2. age from 55 to 75 years for subjects without lung cancer family history; age 50-75 years for subjects with lung cancer family history (age less than 50 but older than the age at diagnosis of the youngest lung cancer proband is also eligible)
  3. Having at least one of the following conditions:

(1)with family history of lung cancer within 1st, 2nd or 3rd degree relatives (2)with exposure history of environmental tobacco smoke in workplace or in home (3)history of chronic lung disease (Tuberculosis or COPD) (4)the cooking index equal or over than 110 [cooking index = 2/7 x (days of cooking by pan frying, stir frying, or deep frying in one week) x (cooking years)] (5)cooking without using cooking ventilation

Exclusion criteria

Exclusion Criteria:

  1. with history of lung cancer, or with cancers except skin cancer or cervical carcinoma in situ in the past 5 years
  2. can not accept invasive diagnostic procedure or surgery
  3. have been examined by chest computed tomography in the past 18 months
  4. have unexplained hemoptysis in one month
  5. weight loss over than 6 kg with unexplained reason among one year
  6. pregnant
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
12,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Non-smokers at risk for lung cancer

    1. Non-smoking subjects with lung cancer family history 2. Non-smoking subjects with a given lung cancer risk other than lung cancer family history

    Other: LDCT

Interventions

  • OtherLDCT

    LDCT at enrollment, annually for two years and biennially for 6 years if no lung cancer is detected

06

What researchers measure

Primary outcomes

  1. Validity of LDCT for lung cancer among non-smokers

    True positive, false positive, true negative and false negative rates of LDCT on lung cancer screening. Each subject who is recognized as high risk to lung cancer will be recruited between 2014-2016.

    Time frame: 3 years

Secondary outcomes

  1. Monitoring the occurrence of lung cancer

    Subjects who are recruited between 2014-2016 in this study will be followed every 3-12 months according to their nodule(s) discovered by LDCT for 5 years to obtain their potential occurrence of lung cancer

    Time frame: 5 years

  2. Monitoring the recurrence of lung cancer

    Subjects who have been diagnosed as lung cancer in this study will be monitored for their potential recurrence of lung cancer after clinical treatments/surgery by 5 years

    Time frame: 5 years

07

Study locations

17 sites
  • Chiayi Chang Gung Memorial Hospital
    Chiayi City, 61363, Taiwan
  • Hualien Tzu Chi Hospital
    Hualien City, Taiwan
  • Kaohsiung Medical University Chung-Ho Memorial Hospital
    Kaohsiung, 807, Taiwan
  • Kaohsiung Veterans General Hospital
    Kaohsiung, 81362, Taiwan
  • Kaohsiung Chang Gung Memorial Hospital
    Kaohsiung, 83301, Taiwan
  • E-Da Cancer Hospital
    Kaohsiung, Taiwan
  • Shuang-Ho Hospital
    New Taipei City, Taiwan
  • Chung Shan Medical University Hospital
    Taichung, 40201, Taiwan
  • China Medical University Hospital
    Taichung, 404, Taiwan
  • Taichung Veterans General Hospital
    Taichung, 407, Taiwan
  • National Cheng Kung University Hospital
    Tainan, Taiwan
  • National Taiwan University Hospital
    Taipei, 112, Taiwan
  • Taipei Veterans General Hospital
    Taipei, 112, Taiwan
  • Tri-Service General Hospital
    Taipei, 114, Taiwan
  • Taipei Medical University Hospital
    Taipei, Taiwan
  • Wan Fang Hospital
    Taipei, Taiwan
  • Linkou Chang Gung Memorial Hospital
    Taoyuan City, 33001, Taiwan
08

References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 30, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02611570
Lead sponsor
Academia Sinica, Taiwan
Collaborators
Taiwan Lung Cancer Society, National Taiwan University Hospital, Taipei Veterans General Hospital, Taiwan, Tri-Service General Hospital, Chang Gung Memorial Hospital, Taichung Veterans General Hospital, Chung Shan Medical University, Kaohsiung Veterans General Hospital., Kaohsiung Medical University Chung-Ho Memorial Hospital, China Medical University Hospital, National Health Research Institutes, Taiwan, Ministry of Health and Welfare, Taiwan
Responsible party
Pan-Chyr Yang, MD, PhD (Research Fellow, Academia Sinica, Taiwan) — Principal investigator
First posted
Nov 23, 2015
Start date
Oct 2014
Primary completion
Jul 2027 (estimated)
Completion
Jul 2028 (estimated)
Last update
Oct 30, 2024

Study contacts

Pan-Chyr Yang, M.D., Ph.D.
principal investigator · National Taiwan University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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